Anti-Fungal Powder
- Product NDC
- 36800-613
- 11-digit product format
- 368000613
- Labeler code
- 36800
- Product ID
- 36800-613_42f4c03f-a3fe-ff3f-e063-6294a90a72df
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- TopCo Associates
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-06-03
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Anti-Fungal Powder
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998461 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36800-613-01 | Anti-Fungal Powder | 71 g in 1 BOTTLE, PLASTIC | POWDER | 71 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-613 | ANTI-FUNGAL POWDER (MICONAZOLE NITRATE) POWDER [TOPCO ASSOCIATES] | 2 | Current NDC, 1 package rows | 20241109_19c3fbc5-abde-57df-e063-6394a90a125c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 36800-613-01 | 36800061301 | 71 g in 1 BOTTLE, PLASTIC (36800-613-01) | 71 g | 2024-06-03 | No | No | Historical |